Basic Salary Up from $4000 to $7,000 + 2 months VB
Working location: West MRT
Pharmaceutical Industry Experience is a MUST
Aseptic technique for QC candidates
CIP, SIP experiences will be preferred
Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process Equipment, CIP / SIP, Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations, Method validation (analytical chemistry, biochemistry, microbiological) & Enterprise system (LIMS, QMS).
Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
Investig6te deviations, write investigation reports and create summary reports.
Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
Bachelor's degree in technical discipline such as Engineering or Science or with experience relevant to the Job Description.
Minimum 3 years of experience in pharmaceutical industry